Unlock the Full Potential of Your Development

Bring together experienced patient experts in clinical development to provide invaluable insights throughout your product development plans.

Our approach: We develop a charter as the foundation, identify and contract with the right participants, and execute the board meetings based on a structured moderation guide.

Your outcomes: A dedicated, ongoing patient advisory board with experienced participants who are knowledgeable, engaged, and ready to share meaningful insights to support all your patient-related questions.

Optimize trial logistics and practical execution, refine your clinical trial design and reduce the burden to participate through direct patient feedback. Make sure your clinical trials do not fail due to unrealistic set-ups.

Our approach: We identify the right patient expert partners, manage contracting, prepare all stakeholders for engagement, and create a safe and respectful environment to openly explore patient perspectives and needs guided by a structured moderation plan.

Your outcomes: A clear report with initial qualitative insights and recommendations that inform your clinical trial design and highlight where additional logistics or adjustments may be needed to ensure patient participation.

Co-create materials, gain qualitative insights and advice on specific topics directly from those living with the disease. Workshops can be in person or virtual with up to 10-12 individuals.

Our approach: We identify the right patients for your specific co-creation activity, manage contracting, and lead the workshop using a clear moderation guide and interactive design-thinking methodologies, enabling an effective creation process, whether virtual or in person.

Your outcomes: A comprehensive report that informs the development of materials such as trial information, patient education tools, adherence-support materials, and other patient-relevant resources based on patients’ perspectives.

Reach those who may benefit from participating in your clinical trials. Spread the word through patient advocacy groups and the whole patient community.

Our approach: We create a dedicated patient-friendly landing page and tailored recruitment materials for social media, patient-organization channels, and community networks. We set up Google Ads campaigns and continuously monitor and optimize them to maximize reach and engagement.

Your outcomes: A faster, more efficient recruitment process supported by regular reports on recruitment metrics, giving you full transparency and control over budget and progress.

Supplement your clinical trial dataset with highly valuable qualitative patient experience data from those who took part. Demonstrate added value to payers, validate your endpoints, and optimize future clinical trial design and execution.

Our approach: We design interviews in alignment with your clinical trial, prepare material for ethics submission, liaise closely with study sites, and establish processes that work smoothly for all stakeholders. We conduct and record the interviews, transcribe and code the data, and analyze the results in full compliance with data privacy requirements and ICH-GCP.

Your outcomes: A comprehensive report ready to be incorporated into dossier development (e.g.for HTA purposes), providing evidence generated directly from the patient perspective.

Include Patient Reported Outcome Measures (PROMs) in your clinical trials or patient insight research to assess patient relevance.

Our approach: We bring in the patient voice for concept validation and testing of PROMs. Using both qualitative and quantitative methods, we support the full validation process with robust patient insights, ensuring feasibility, clarity, and true patient relevance.

Your outcomes: A qualitative and/or quantitative insights report that directly supports the PROM validation process in accordance with FDA guidelines.

Gain a deep understanding of the needs and priorities of people living with the disease to demonstrate patient-relevant endpoints in regulatory and HTA decision-making processes.

Our approach: We thoroughly analyze the full decision context, then select the most appropriate qualitative (e.g., interviews) and/or quantitative (e.g., Discrete-Choice Experiments) methodologies for your objectives. All development and execution follow the latest guidelines from IMI PREFER, ISPOR, and the FDA.

Your outcomes: High-quality insights that are ready for publication or internal decision-making, revealing patient needs and priorities that can be applied across multiple areas such as target product profiles, endpoint selection, and many other strategic decisions.

Conduct interviews and surveys to better understand patient pathways, burden of disease or unmet medical needs. Collect patient experience data which enrich your clinical trial outcomes with real-world insights.

Our approach: Using qualitative methods (e.g., in-depth or semi-structured interviews and focus groups) and quantitative approaches (e.g., online surveys), we gather robust patient experience data. We co-create study elements with patients and HCPs, collect and analyze the data, all while following the latest guidance from the FDA (PFDD) and PFMD.

Your outcomes: A comprehensive report that can be used for medical writing of scientific publications or internal decision-making plus an executive summary and supplementary analytical files.